Towards clinical translation of ligand-functionalized liposomes in targeted cancer therapy: Challenges and opportunities

L Belfiore, DN Saunders, M Ranson… - Journal of controlled …, 2018 - Elsevier
The development of therapeutic resistance to targeted anticancer therapies remains a
significant clinical problem, with intratumoral heterogeneity playing a key role. In this context …

Survivin small molecules inhibitors: recent advances and challenges

N Albadari, W Li - Molecules, 2023 - mdpi.com
Survivin, as a member of the inhibitor of apoptosis proteins (IAPs) family, acts as a
suppressor of apoptosis and plays a central role in cell division. Survivin has been …

Long non-coding RNAs (lncRNAs) signaling in cancer chemoresistance: from prediction to druggability

GC Eptaminitaki, D Stellas, B Bonavida… - Drug Resistance Updates, 2022 - Elsevier
The acquisition of cancer cell resistance to conventional chemotherapeutics is considered
the major driver of treatment failure and disease recurrence in most solid and hematological …

Characterization of cancer genomic heterogeneity by next-generation sequencing advances precision medicine in cancer treatment

J Zhang, SS Späth, SL Marjani… - Precision clinical …, 2018 - academic.oup.com
Cancer is a heterogeneous disease with unique genomic and phenotypic features that differ
between individual patients and even among individual tumor regions. In recent years, large …

Using genome sequence to enable the design of medicines and chemical probes

AJ Angelbello, JL Chen, JL Childs-Disney… - Chemical …, 2018 - ACS Publications
Rapid progress in genome sequencing technology has put us firmly into a postgenomic era.
A key challenge in biomedical research is harnessing genome sequence to fulfill the …

Tyrosine kinase inhibitors as modulators of ATP binding cassette multidrug transporters: substrates, chemosensitizers or inducers of acquired multidrug resistance?

A Brózik, C Hegedüs, Z Erdei, T Hegedűs… - Expert opinion on …, 2011 - Taylor & Francis
Introduction: Anticancer tyrosine kinase inhibitors (TKIs) are small molecule hydrophobic
compounds designed to arrest aberrant signaling pathways in malignant cells. Multidrug …

Genetic mutations and epigenetic modifications: driving cancer and informing precision medicine

KM Coyle, JE Boudreau… - BioMed research …, 2017 - Wiley Online Library
Cancer treatment is undergoing a significant revolution from “one‐size‐fits‐all” cytotoxic
therapies to tailored approaches that precisely target molecular alterations. Precision …

Management of chronic myeloid leukaemia: current treatment options, challenges, and future strategies

S Younes, MA Ismail, R Al-Jurf, A Ziyada… - …, 2023 - Taylor & Francis
Small molecule therapy is a critical component of targeted anticancer treatment, with
tyrosine kinase inhibitors (TKIs) being the first compounds to treat the clonal Chronic …

[HTML][HTML] The first pentacyclic triterpenoid gypsogenin derivative exhibiting anti-ABL1 kinase and anti-chronic myelogenous leukemia activities

HI Ciftci, SE Ozturk, TFS Ali, MO Radwan… - Biological and …, 2018 - jstage.jst.go.jp
The discovery of the chimeric tyrosine kinase breakpoint cluster region kinase-Abelson
kinase (BCR-ABL)-targeted drug imatinib conceptually changed the treatment of chronic …

Secretion of IL‐1β from imatinib‐resistant chronic myeloid leukemia cells contributes to BCRABL mutation‐independent imatinib resistance

CR Lee, JA Kang, HE Kim, Y Choi, T Yang… - FEBS …, 2016 - Wiley Online Library
Some cases of chronic myelogenous leukemia are resistant to tyrosine kinase inhibitors (TKI
s) independently of mutation in BCR–ABL, but the detailed mechanism underlying this …